Lobetyolin |
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Catalog No.GN10569
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Lobetyolin is a derivative of lobetyol substituted with a glucopyranose.
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 136085-37-5
Sample solution is provided at 25 µL, 10mM.
Lobetyolin is a derivative of lobetyol substituted with a glucopyranose[1]. Lobetyolin is an important polyacetylene in Codonopsis Radix, which is of great interest on account of its unique chemical structures as well as its potential physiological functions. As suggested by extensive studies, Lobetyolin shows diverse functions such as antioxidant, anti-inflammatory, and immunomodulatory activities, especially antitumor activity, which may be due to the strong affinity of polyacetylenes to bind to proteins serving as the natural receptors of Michael response. Lobetyolin greatly impaired the proliferation of PC-3 cells, with corresponding IC50 values of 5.73μM[2].
In vitro, epithelial cells derived from human embryonic kidney were treated with a gradient of different Lobetyolin concentrations (5, 10, 15, 20, 25, 30μM) for 24 hours, followed by treatment with cisplatin at a concentration of 20µM. The experimental results demonstrate that Lobetyolin exhibits a dose-dependent cytoprotective effect against cisplatin-induced toxicity in HEK293 cells, establishing it as an effective cytoprotective agent[3]. Pre-treatment with Lobetyolin (1, 10, and 100µM) for 30 minutes, followed by stimulation with phorbol 12-myristate 13-acetate (PMA, 10ng/mL) for 24 hours in NCI-H292 cells, significantly inhibited the expression of MUC5AC gene induced by PMA[4].
In vivo, 10mM Lobetyolin with intraperitoneal injections treatment in mice demonstrated a remarkable reduction in the production of IL-6, TNF-α, and IL-1β in the serum, along with mitigated lung and liver tissue damage characterized by reduced inflammatory cell infiltration[5]. Lobetyolin, when administered intraperitoneally at doses of 10, 20, and 40mg/kg for two weeks, significantly reduced tumor volume and markedly decreased the expression of Alanine, Serine, Cysteine-Preferring Transporter 2 (ASCT2) mRNA in mice. These results suggest that Lobetyolin exhibits anti-cancer effects in nude mice, possibly through the inhibition of glutamine metabolism[6].
Reference:
[1] Bailly C. Anticancer Properties of Lobetyolin, an Essential Component of Radix Codonopsis (Dangshen). Nat Prod Bioprospect. 2021;11(2):143-153.
[2] Xie Q, Wang H, Guan H, et al. The in vitro/in vivo metabolic pathways analysis of lobetyol, lobetyolin, and lobetyolinin, three polyacetylenes from Codonopsis Radix, by UHPLC-Q/TOF-MS and UHPLC-MS/MS. J Pharm Biomed Anal. 2023;223:115140.
[3] Hou YY, Qi SM, Leng J, et al. Lobetyolin, a Q-marker isolated from Radix Platycodi, exerts protective effects on cisplatin-induced cytotoxicity in HEK293 cells. J Nat Med. 2023;77(4):721-734.
[4] Yoon YP, Ryu J, Park SH, et al. Effects of Lobetyolin, Lobetyol and Methyl linoleate on Secretion, Production and Gene Expression of MUC5AC Mucin from Airway Epithelial Cells. Tuberc Respir Dis (Seoul). 2014;77(5):203-208.
[5] Chen Z, Su Y, Ding J, He J, Lai L, Song Y. Lobetyolin protects mice against LPS-induced sepsis by downregulating the production of inflammatory cytokines in macrophage. Front Pharmacol. 2024;15:1405163.
[6] He W, Tao W, Zhang F, et al. Lobetyolin induces apoptosis of colon cancer cells by inhibiting glutamine metabolism. J Cell Mol Med. 2020;24(6):3359-3369.
| Cell experiment [1]: | |
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Cell lines |
epithelial cells derived from human embryonic kidney |
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Preparation Method |
HEK293, an epithelial cell derived from the human embryonic kidney cell line, was cultured in Dulbecco’s modified eagle’s medium (DMEM) supplemented with 10% fetal bovine serum (FBS). Following a 24h treatment with varying concentrations of Lobetyolin, the cells will subsequently undergo cisplatin treatment at a concentration of 20µM. |
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Reaction Conditions |
5, 10, 15, 20, 25, 30μM; 24h |
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Applications |
The experimental results demonstrate that Lobetyolin exhibits a dose-dependent cytoprotective effect against cisplatin-induced toxicity in HEK293 cells, establishing it as an effective cytoprotective agent. |
| Animal experiment [2]: | |
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Animal models |
BALB/c female nude mice (5–6 weeks) weighing ~ 20g |
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Preparation Method |
0.1mL cell suspension containing about 5 × 106 MKN-45 cells was injected subcutaneously into the right flank region. The Lobetyolin-treated group was given saline containing 10mg/kg Lobetyolin once per day, and the control group was given the same volume of saline once per day. The tumors were administered every five days, and the tumor size was measured simultaneously to plot the growth curve. The tumor growth was monitored by measuring tumor volume. After 30 days, mice were euthanized by cervical dislocation to dissect the tumor tissues. |
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Dosage form |
10mg/kg; subcutaneously injected |
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Applications |
Lobetyolin showed a significant anti-tumor effect in cancer cell xenograft models. The expression levels of ASCT2 and Ki67 were significantly reduced in the Lobetyolin group compared to the control group. |
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Reference: |
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| Cas No. | 136085-37-5 | SDF | |
| Chemical Name | (2R,3R,4S,5S,6R)-2-[(4E,12E)-1,7-dihydroxytetradeca-4,12-dien-8,10-diyn-6-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol | ||
| Canonical SMILES | CC=CC#CC#CC(C(C=CCCCO)OC1C(C(C(C(O1)CO)O)O)O)O | ||
| Formula | C20H28O8 | M.Wt | 396.43 |
| Solubility | ≥ 17.4mg/mL in EtOH;50mg/ml in DMSO | Storage | Store at -20°C,protect from light |
| General tips | Please select the appropriate solvent to prepare the stock solution according to the
solubility of the product in different solvents; once the solution is prepared, please store it in
separate packages to avoid product failure caused by repeated freezing and thawing.Storage method
and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored
at -20°C, please use it within 1 month. To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time. |
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| Shipping Condition | Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request. | ||
| Prepare stock solution | |||
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1 mg | 5 mg | 10 mg |
| 1 mM | 2.5225 mL | 12.6126 mL | 25.2251 mL |
| 5 mM | 504.5 μL | 2.5225 mL | 5.045 mL |
| 10 mM | 252.3 μL | 1.2613 mL | 2.5225 mL |
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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )
Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL saline, mix and clarify.
Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.
Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such as vortex, ultrasound or hot water bath can be used to aid dissolving.
3. All of the above co-solvents are available for purchase on the GlpBio website.
Quality Control & SDS
- View current batch:
- Purity: >98.00% Appearance: A solid
- COA (Certificate of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
Average Rating: 5 (Based on Reviews and 30 reference(s) in Google Scholar.)















